Maize inbred PH2DMA

ABSTRACT

A novel maize variety designated PH2DMA and seed, plants and plant parts thereof are provided. Methods for producing a maize plant comprise crossing maize variety PH2DMA with another maize plant. Methods for producing a maize plant containing in its genetic material one or more traits introgressed into PH2DMA through backcross conversion and/or transformation, and to the maize seed, plant and plant part produced thereby are provided. Hybrid maize seed, plants or plant parts are produced by crossing the variety PH2DMA or a locus conversion of PH2DMA with another maize variety.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. §119 to provisional application Ser. No. 62/114,617 filed Feb. 11, 2015, herein incorporated by reference in its entirety.

FIELD OF THE INVENTION

This invention relates generally to the field of maize, Zea mays L., breeding, and to an inbred maize variety designated PH2DMA.

BACKGROUND

The goal of plant breeding is to combine, in a single variety or hybrid, various desirable traits. For field crops, these traits may include resistance to diseases and insects, resistance to heat and drought, reducing the time to crop maturity, greater yield, and better agronomic quality. Increased uniformity of plant characteristics such as germination, stand establishment, growth rate, maturity, plant height and ear height can expedite mechanical harvesting of many crops. Traditional plant breeding facilitates the development of new and improved crops.

SUMMARY

Provided is a novel maize, Zea mays L., variety, designated PH2DMA and processes for making PH2DMA. In certain embodiments, seeds of maize variety PH2DMA, plants of maize variety PH2DMA, plant parts of maize variety PH2DMA, and processes for making a maize plant that comprise crossing maize variety PH2DMA with another maize plant are provided. Processes for making a maize plant containing in its genetic material one or more traits introgressed into PH2DMA through backcross conversion, transformation, or both and to the maize seed, plant and plant parts produced thereby are also disclosed. In certain embodiments, a hybrid maize seed, plant or plant part produced by crossing the variety PH2DMA or a locus conversion of PH2DMA with another maize variety is provided.

DEFINITIONS

Certain definitions used in the specification are provided below. Also in the examples that follow, a number of terms are used herein. In order to provide a clear and consistent understanding of the specification and claims, including the scope to be given such terms, the following definitions are provided. NOTE: ABS is in absolute terms and % MN is percent of the mean for the experiments in which the inbred or hybrid was grown. PCT designates that the trait is calculated as a percentage. % NOT designates the percentage of plants that did not exhibit a trait. For example, STKLDG % NOT is the percentage of plants in a plot that were not stalk lodged. These designators will follow the descriptors to denote how the values are to be interpreted. Below are the descriptors used in the data tables included herein.

ABIOTIC STRESS TOLERANCE: resistance to non-biological sources of stress conferred by traits such as nitrogen utilization efficiency, altered nitrogen responsiveness, drought resistance, cold, and salt resistance

ABTSTK=ARTIFICIAL BRITTLE STALK: A count of the number of “snapped” plants per plot following machine snapping. A snapped plant has its stalk completely snapped at a node between the base of the plant and the node above the ear. Artificial brittle stalk is expressed as percent of plants that did not snap.

ANT ROT=ANTHRACNOSE STALK ROT (Colletotrichum graminicola): A 1 to 9 visual rating indicating the resistance to Anthracnose Stalk Rot. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

BACKCROSSING: Process in which a breeder crosses a hybrid or other progeny variety back to one of the parental genotypes one or more times.

BARPLT=BARREN PLANTS: The percent of plants per plot that were not barren (lack ears).

BLUP=BEST LINEAR UNBIASED PREDICTION. The BLUP values are determined from a mixed model analysis of hybrid performance observations at various locations and replications. BLUP values for inbred maize plants, breeding values, are estimated from the same analysis using pedigree information.

BORBMN=ARTIFICIAL BRITTLE STALK MEAN: The mean percent of plants not “snapped” in a plot following artificial selection pressure. A snapped plant has its stalk completely snapped at a node between the base of the plant and the node above the ear. Expressed as percent of plants that did not snap. A high number is good and indicates tolerance to brittle snapping.

BRENGMN=BRITTLE STALK ENERGY MEAN: The mean amount of energy per unit area needed to artificially brittle snap a corn stalk. A high number is good and indicates tolerance to brittle snapping.

BREEDING VALUE: A relative value determined by evaluating the progeny of the parent. For corn the progeny is often the F1 generation and the parent is often an inbred variety.

BRLPNE=ARTIFICIAL ROOT LODGING EARLY SEASON: The percent of plants not root lodged in a plot following artificial selection pressure applied prior to flowering. A plant is considered root lodged if it leans from the vertical axis at an approximately 30 degree angle or greater. Expressed as percent of plants that did not root lodge. A high number is good and indicates tolerance to root lodging.

BRLPNL=ARTIFICIAL ROOT LODGING LATE SEASON: The percent of plants not root lodged in a plot following artificial selection pressure during grain fill. A plant is considered root lodged if it leans from the vertical axis at an approximately 30 degree angle or greater. Expressed as percent of plants that did not root lodge. A high number is good and indicates tolerance to root lodging.

BRTSTK=BRITTLE STALKS: This is a measure of the stalk breakage near the time of pollination, and is an indication of whether a hybrid or inbred would snap or break near the time of flowering under severe winds. Data are presented as percentage of plants that did not snap. Data are collected only when sufficient selection pressure exists in the experiment measured.

BRTPCN=BRITTLE STALKS: This is an estimate of the stalk breakage near the time of pollination, and is an indication of whether a hybrid or inbred would snap or break near the time of flowering under severe winds. Data are presented as percentage of plants that did not snap. Data are collected only when sufficient selection pressure exists in the experiment measured.

CELL: Cell as used herein includes a plant cell, whether isolated, in tissue culture or incorporated in a plant, seed or plant part.

CLDTST=COLD TEST: The percent of plants that germinate under cold test conditions.

CLN=CORN LETHAL NECROSIS: Synergistic interaction of maize chlorotic mottle virus (MCMV) in combination with either maize dwarf mosaic virus (MDMV-A or MDMV-B) or wheat streak mosaic virus (WSMV). A 1 to 9 visual rating indicating the resistance to Corn Lethal Necrosis. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

CMSMT=COMMON SMUT: This is the percentage of plants not infected with Common Smut. Data are collected only when sufficient selection pressure exists in the experiment measured.

COMRST=COMMON RUST (Puccinia sorghi): A 1 to 9 visual rating indicating the resistance to Common Rust. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

D and D1-Dn: represents the generation of doubled haploid.

D/D=DRYDOWN: This represents the relative rate at which a hybrid will reach acceptable harvest moisture compared to other hybrids on a 1 to 9 rating scale. A high score indicates a hybrid that dries relatively fast while a low score indicates a hybrid that dries slowly.

DIGENG=DIGESTIBLE ENERGY: Near-infrared transmission spectroscopy, NIT, prediction of digestible energy.

DIPERS=DIPLODIA EAR MOLD SCORES (Diplodia maydis and Diplodia macrospora): A 1 to 9 visual rating indicating the resistance to Diplodia Ear Mold. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

DIPROT=DIPLODIA STALK ROT SCORE: Score of stalk rot severity due to Diplodia (Diplodia maydis). Expressed as a 1 to 9 score with 9 being highly resistant. Data are collected only when sufficient selection pressure exists in the experiment measured.

DRPEAR=DROPPED EARS: A measure of the number of dropped ears per plot and represents the percentage of plants that did not drop ears prior to harvest. Data are collected only when sufficient selection pressure exists in the experiment measured.

D/T=DROUGHT TOLERANCE: This represents a 1 to 9 rating for drought tolerance, and is based on data obtained under stress conditions. A high score indicates good drought tolerance and a low score indicates poor drought tolerance. Data are collected only when sufficient selection pressure exists in the experiment measured.

EARMLD=GENERAL EAR MOLD: Visual rating (1 to 9 score) where a 1 is very susceptible and a 9 is very resistant. This is based on overall rating for ear mold of mature ears without determining the specific mold organism, and may not be predictive for a specific ear mold. Data are collected only when sufficient selection pressure exists in the experiment measured.

EBTSTK=EARLY BRITTLE STALK: A count of the number of “snapped” plants per plot following severe winds when the corn plant is experiencing very rapid vegetative growth in the V5-V8 stage. Expressed as percent of plants that did not snap. Data are collected only when sufficient selection pressure exists in the experiment measured.

ECB1LF=EUROPEAN CORN BORER FIRST GENERATION LEAF FEEDING (Ostrinia nubilalis): A 1 to 9 visual rating indicating the resistance to preflowering leaf feeding by first generation European Corn Borer. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

ECB2IT=EUROPEAN CORN BORER SECOND GENERATION INCHES OF TUNNELING (Ostrinia nubilalis): Average inches of tunneling per plant in the stalk. Data are collected only when sufficient selection pressure exists in the experiment measured.

ECB2SC=EUROPEAN CORN BORER SECOND GENERATION (Ostrinia nubilalis): A 1 to 9 visual rating indicating post flowering degree of stalk breakage and other evidence of feeding by second generation European Corn Borer. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

ECBDPE=EUROPEAN CORN BORER DROPPED EARS (Ostrinia nubilalis): Dropped ears due to European Corn Borer. Percentage of plants that did not drop ears under second generation European Corn Borer infestation. Data are collected only when sufficient selection pressure exists in the experiment measured.

ECBLSI=EUROPEAN CORN BORER LATE SEASON INTACT (Ostrinia nubilalis): A 1 to 9 visual rating indicating late season intactness of the corn plant given damage (stalk breakage above and below the top ear) caused primarily by 2^(nd) and/or 3^(rd) generation ECB larval feeding before harvest. A higher score is good and indicates more intact plants. Data are collected only when sufficient selection pressure exists in the experiment measured.

EDANTCOLs=ANTHER COLOR: Rated on a 1 to 7 scale where 1 is green, 2 is yellow, 3 is pink, 5 is red, and 7 is purple.

EDantants=ANTHER ANTHOCYANIN COLOR INTENSITY: A measure of anther anthocyanin color intensity rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Observed in the middle third of the main branch on fresh anthers.

EDbarants=GLUME ANTHOCYANIN COLORATION AT BASE (WHOLE PLANT, EAR INSERTION LEVEL): A measure of the color intensity at the base of the glume, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Observed in the middle third of the main branch of the tassel.

EDBARCOLs=BAR GLUME COLOR INTENSITY: A measure of the bar glume color intensity. Bar glume is a dark purple band that may occur on the bottom of a glume. Bar glume color intensity is measured on a scale of 1 to 7 where 1 is absent, 2 is weak, 3 is medium, 5 is strong, and 7 is very strong.

EDBRROANTs=BRACE ROOTS ANTHOCYANIN COLORATION: A measure of the color intensity of the brace roots rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Observed when well developed and fresh brace roots are present on 50% of plants.

EDCOBAINTs=COB GLUME ANTHOCYANIN COLOR INTENSITY: Rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Anthocyanin coloration should be observed on the middle third of the uppermost cob, after the removal of some of the grains.

EDCOBCOLs=COB COLOR: A measure of the intensity of pink or salmon coloration of the cob, rated on a 1 to 9 scale where 1 is absent or white, 2 is light pink, 3 is pink, 4 is medium red, 5 is red, 6 is medium red, 7 is dark red, 8 is dark to very dark red, and 9 is present.

EDCOBDIA=COB DIAMETER: Measured in mm.

EDCOBICAs=COB ANTHOCYANIN COLOR INTENSITY: A measure of the intensity of pink or salmon coloration of the cob, rated on a 1 to 9 scale where 1 is very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong.

EDDAYSH=NUMBER OF DAYS TO SHEDDING FROM PLANTING: The number of growing degree units (GDUs) or heat units required for an inbred variety or hybrid to have approximately 50 percent of the plants shedding pollen and is measured from the time of planting. Growing degree units are calculated by the Barger Method, where the heat units for a 24-hour period are:

${G\; D\; U} = {\frac{\left( {{Max}.\mspace{14mu}{temp}.\;{+ \;{{Min}.\mspace{14mu}{temp}.}}} \right)}{2} - 50}$

The units determined by the Barger Method are then divided by 10. The highest maximum temperature used is 86 degrees F., and the lowest minimum temperature used is 50 degrees F. For each inbred or hybrid it takes a certain number of GDUs to reach various stages of plant development.

EDDAYSLK=NUMBER OF DAYS TO SILKING FROM PLANTING: The number of growing degree units required for an inbred variety or hybrid to have approximately 50 percent of the plants with silk emergence from time of planting. Growing degree units are calculated by the Barger Method as given in EDDAYSH definition and then divided by 10.

EDEARDIA=EAR DIAMETER: Measured in mm.

EDEARHT=EAR HEIGHT: A measure from the ground to the highest placed developed ear node attachment, measured in centimeters.

EDEARHULs=EAR HUSK LENGTH: A measure of ear husk length rated on a 1 to 9 scale where 1 is very short, 3 is short, 5 is medium, 7 is long, and 9 is very long.

EDEARLNG=EAR LENGTH: Measured in mm.

EDEARROW=NUMBER OF ROWS OF GRAIN ON EAR.

EDEARSHAs=EAR SHAPE (TAPER): Rated on a 1 to 3 scale where 1 is conical, 2 is conico-cylindrical, and 3 is cylindrical.

EDEARSHLs=EAR SHANK LENGTH SCALE: A measure of the length of the ear shank or peduncle, rated on a 1 to 9 scale where 1 is very short, 3 is short, 5 is medium, 7 is long, 9 is very long.

EDFILEANs=SHEATH ANTHOCYANIN COLOR INTENSITY AT FIRST LEAF STAGE: A measure of the anthocyanin color intensity of the sheath of the first leaf, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong.

EDFILECOs=FOLIAGE INTENSITY OF GREEN COLOR: A measure of the green coloration intensity in the leaves, rated on a 1 to 3 scale where 1 is light, 2 is medium, and 3 is dark.

EDFILESHs=LEAF TIP SHAPE: An indication of the shape of the apex of the first leaf, rated on a 1 to 5 scale where 1 is pointed, 2 is pointed to rounded, 3 is rounded, 4 is rounded to spatulate, and 5 is spatulate.

EDGLUANTs=GLUME ANTHOCYANIN COLOR EXCLUDING BASE: A measure of the color intensity of the glume excluding the base, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Observed in the middle third of the main branch of the tassel.

EDGLUCOLs=GLUME COLOR: Rated on a 1 to 7 scale where 1 is green, 2 is yellow, 3 is pink, 5 is red, and 7 is purple.

EDKERDOCs=DORSAL SIDE OF GRAIN COLOR: Rated on a 1 to 10 scale where 1 is white, 2 is yellowish white, 3 is yellow, 4 is yellow orange, 5 is orange, 6 is red orange, 7 is red, 8 is purple, 9 is brownish, and 10 is blue black. Observed in the middle third of the uppermost ear when well developed.

EDKERSHAs=KERNEL SHAPE: Rated on a 1 to 3 scale where 1 is round, 2 is kidney-shaped, and 3 is cuneiform.

EDKERTCOs=TOP OF GRAIN COLOR: Rated on a 1 to 10 scale where 1 is white, 2 is yellowish white, 3 is yellow, 4 is yellow orange, 5 is orange, 6 is red orange, 7 is red, 8 is purple, 9 is brownish, and 10 is blue black. Observed in the middle third of the uppermost ear when well developed.

EDKERTYPs=TYPE OF GRAIN: Observed in the middle third of the uppermost ear when well developed. Rated on a 1 to 9 scale where 1 is flint (mostly hard endosperm, round grain, thick layer of hard endosperm on crown, larger grains than pop), 2 is flint-like (mostly hard endosperm, round grain, intermediate layer of hard endosperm on crown), 3 is intermediate (thin layer of hard endosperm on crown, crown slightly indented), 4 is dent-like (mostly soft endosperm, crown moderately indented, medium layer of hard endosperm on dorsal side of grain), 5 is dent (mostly soft endosperm covering also exterior part of crown, thin layer of hard endosperm only on dorsal side of grain, grain strongly indented on crown), 6 is sweet (glassy endosperm with very low or no starch content, wrinkled grain), 7 is pop (nearly completely hard endosperm, rice-type (pointed grain) or pearl type (rounded grain), very thick layer of hard endosperm on crown, smaller grains than flint), 8 is waxy (approximately 100% amylopectin, waxy appearance of grain, pink coloration of endosperm in iodine staining test), 9 is flour (completely soft endosperm, grain round or slightly indented on crown.

EDLEAANGs=LEAF ANGLE BETWEEN BLADE AND STEM: A measure of the angle formed between stem and leaf, rated on a 1 to 9 scale where 1 is very small (<5 degrees), 3 is small (6 to 37 degrees), 5 is medium (38 to 62 degrees), 7 is large (63 to 90 degrees), and 9 is very large (>90 degrees). Observed on the leaf just above the upper ear.

EDLEAATTs=LEAF ATTITUDE OF ENTIRE PLANT: A measure of leaf curvature or attitude, rated on a 1 to 9 scale where 1 is absent or very slightly recurved, 3 is slightly recurved, 5 is moderately recurved, 7 is strongly recurved, and 9 is very strongly recurved. Observed on the leaf just above the upper ear.

EDLEALNGs=LEAF LENGTH SCORE: A measure of leaf length rated on a 1 to 9 scale where 1 indicates <0.70 m, 3 indicates 0.70 m to 0.80 m, 5 indicates 0.80 m to 0.90 m, 7 indicates 0.90 m to 1 m, and 9 indicates >1.00 m.

EDLEAWID=LEAF WIDTH OF BLADE: A measure of the average leaf width in centimeters.

EDLELIANTs=LEAF LIMB ANTHOCYANIN COLOR INTENSITY OF ENTIRE PLANT: A measure of the leaf limb anthocyanin coloration, rated on a 1 to 9 scale with 1 being absent or very weak, 3 being weak, 5 being medium, 7 being strong, and 9 being very strong.

EDNODANTS=NODES ANTHOCYANIN COLOR INTENSITY: A measure of the anthocyanin coloration of nodes, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong.

EDPLTHWT=PLANT HEIGHT WITH TASSEL: A measure of the height of the plant from the ground to the tip of the tassel in centimeters.

EDRATIOEP=RATIO HEIGHT OF INSERTION OF PEDUNCLE OF UPPER EAR TO PLANT LENGTH.

EDSHEAHAs=LEAF SHEATH HAIRNESS SCALE: Rated on a 1 to 6 scale where 1 indicates none and 6 indicates fuzzy.

EDSHEAANTs=SHEATH ANTHOCYANIN COLOR INTENSITY: Rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong.

EDSLKAINTs=SILK ANTHOCYANIN COLOR INTENSITY: A measure of the color intensity of the silks, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong.

EDSTLANTs=INTERNODE ANTHOCYANIN COLOR INTENSITY: A measure of anthocyanin coloration of nodes, rated on a 1 to 9 scale where 1 is absent or very weak, 3 is weak, 5 is medium, 7 is strong, and 9 is very strong. Observed just above the insertion point of the peduncle of the upper ear.

EDTA1RYATs=TASSEL LATERAL BRANCH CURVATURE: Rated on a 1 to 9 scale where 1 indicates absent or very slightly recurved (<5 degrees), 3 indicates slightly recurved (6 to 37 degrees), 5 indicates moderately recurved (38 to 62 degrees), 7 indicates strongly recurved (63 to 90 degrees), and 9 indicates very strongly recurved (>90 degrees). Observed on the second branch from the bottom of the tassel.

EDTA1 RYBRs=NUMBER OF PRIMARY LATERAL TASSEL BRANCHES: Rated on a 1 to 9 scale where 1 indicates absent or very few (<4 branches), 3 indicates few (4 to 10), 5 indicates medium (11 to 15), 7 indicates many (16 to 20), and 9 indicates very many (>20).

EDTASAFDs=TASSEL SPIKELET DENSITY: Rated on a 3 to 7 scale where 3 is moderately lax, 5 is medium, and 7 is moderately dense. Observed in the middle third of the main branch of the tassel.

EDTASAHB=LENGTH OF MAIN AXIS ABOVE HIGHEST LATERAL BRANCH: The length of the tassel's main axis above the highest lateral branch in centimeters.

EDTASANGs=TASSEL ANGLE BETWEEN MAIN AXIS AND LATERAL BRANCHES: Rated on a 1 to 9 scale where 1 is very small (<5 degrees), 3 is small (6 to 37 degrees), 5 is medium (38 to 62 degrees), 7 is large (63 to 90 degrees), and 9 is very large (>90 degrees). Observed on the second branch from the bottom of the tassel.

EDTASEBRs=SECONDARY TASSEL BRANCHES (NUMBER): The number of secondary tassel branches, rated on a 1 to 7 scale where 1 indicates 0 to 3 branches, 2 indicates 4 to 10, 3 indicates 11 to 15, 5 indicates 16 to 20, and 7 indicates >20.

EDTASLPBRs=PRIMARY TASSEL BRANCH LENGTH: A measure of the length of the primary or lateral tassel branch, rated on a 1 to 9 scale where 1 is very short, 3 is short, 5 is medium, 7 is long, 9 is very long. Observed on the second branch from the bottom of the tassel.

EDTASULB=LENGTH OF MAIN AXIS ABOVE LOWEST LATERAL BRANCH: The length of the tassel's main axis above the lowest lateral branch in centimeters.

EDZIGZAGs=DEGREE OF STEM ZIG-ZAG: Rated on a scale of 1 to 3 where 1 is absent or very slight, 2 is slight, and 3 is strong.

EGRWTH=EARLY GROWTH: This is a measure of the relative height and size of a corn seedling at the 2-4 leaf stage of growth. This is a visual rating (1 to 9), with 1 being weak or slow growth, 5 being average growth and 9 being strong growth. Taller plants, wider leaves, more green mass and darker color constitute higher score. Data are collected only when sufficient selection pressure exists in the experiment measured.

ERTLDG=EARLY ROOT LODGING: The percentage of plants that do not root lodge prior to or around anthesis; plants that lean from the vertical axis at an approximately 30 degree angle or greater would be counted as root lodged. Data are collected only when sufficient selection pressure exists in the experiment measured.

ERTLPN=EARLY ROOT LODGING: An estimate of the percentage of plants that do not root lodge prior to or around anthesis; plants that lean from the vertical axis at an approximately 30 degree angle or greater would be considered as root lodged. Data are collected only when sufficient selection pressure exists in the experiment measured.

ERTLSC=EARLY ROOT LODGING SCORE: Score for severity of plants that lean from a vertical axis at an approximate 30 degree angle or greater which typically results from strong winds prior to or around flowering recorded within 2 weeks of a wind event. Expressed as a 1 to 9 score with 9 being no lodging. Data are collected only when sufficient selection pressure exists in the experiment measured.

ESTCNT=EARLY STAND COUNT: This is a measure of the stand establishment in the spring and represents the number of plants that emerge on per plot basis for the inbred or hybrid.

EXTSTR=EXTRACTABLE STARCH: Near-infrared transmission spectroscopy, NIT, prediction of extractable starch.

EYESPT=EYE SPOT (Kabatiella zeae or Aureobasidium zeae): A 1 to 9 visual rating indicating the resistance to Eye Spot. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

F1 PROGENY: A progeny plant produced by crossing a plant of one maize line with a plant of another maize line.

FUSERS=FUSARIUM EAR ROT SCORE (Fusarium moniliforme or Fusarium subglutinans): A 1 to 9 visual rating indicating the resistance to Fusarium Ear Rot. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

GDU=GROWING DEGREE UNITS: Using the Barger Heat Unit Theory, which assumes that maize growth occurs in the temperature range 50 degrees F.-86 degrees F. and that temperatures outside this range slow down growth; the maximum daily heat unit accumulation is 36 and the minimum daily heat unit accumulation is 0. The seasonal accumulation of GDU is used in determining maturity zones.

GIBERS=GIBBERELLA EAR ROT (PINK MOLD) (Gibberella zeae): A 1 to 9 visual rating indicating the resistance to Gibberella Ear Rot. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

GIBROT=GIBBERELLA STALK ROT SCORE: Score of stalk rot severity due to Gibberella (Gibberella zeae). Expressed as a 1 to 9 score with 9 being highly resistant. Data are collected only when sufficient selection pressure exists in the experiment measured.

GLFSPT=GRAY LEAF SPOT (Cercospora zeae-maydis): A 1 to 9 visual rating indicating the resistance to Gray Leaf Spot. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

GOSWLT=GOSS' WILT (Corynebacterium nebraskense): A 1 to 9 visual rating indicating the resistance to Goss' Wilt. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

GRNAPP=GRAIN APPEARANCE: This is a 1 to 9 rating for the general appearance of the shelled grain as it is harvested based on such factors as the color of harvested grain, any mold on the grain, and any cracked grain. High scores indicate good grain visual quality.

H and H1: Refers to the haploid generation.

HCBLT=HELMINTHOSPORIUM CARBONUM LEAF BLIGHT (Helminthosporium carbonum): A 1 to 9 visual rating indicating the resistance to Helminthosporium infection. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

HD SMT=HEAD SMUT (Sphacelotheca reiliana): This indicates the percentage of plants not infected. Data are collected only when sufficient selection pressure exists in the experiment measured.

HSKCVR=HUSK COVER: A 1 to 9 score based on performance relative to key checks, with a score of 1 indicating very short husks, tip of ear and kernels showing; 5 is intermediate coverage of the ear under most conditions, sometimes with thin husk; and a 9 has husks extending and closed beyond the tip of the ear. Scoring can best be done near physiological maturity stage or any time during dry down until harvested.

HTFRM=Near-infrared transmission spectroscopy, NIT: prediction of fermentables.

INC D/A=GROSS INCOME (DOLLARS PER ACRE): Relative income per acre assuming drying costs of two cents per point above 15.5 percent harvest moisture and current market price per bushel.

INCOME/ACRE: Income advantage of hybrid to be patented over other hybrid on per acre basis.

INC ADV=GROSS INCOME ADVANTAGE: Gross income advantage of variety #1 over variety #2.

KERUNT=KERNELS PER UNIT AREA (Acres or Hectares).

KERPOP=KERNEL POP SCORE: The visual 1-9 rating of the amount of rupturing of the kernel pericarp at an early stage in grain fill. A higher score is good and indicates no popped (ruptured) kernels.

KER_WT=KERNEL NUMBER PER UNIT WEIGHT (Pounds or Kilograms): The number of kernels in a specific measured weight; determined after removal of extremely small and large kernels.

KSZDCD=KERNEL SIZE DISCARD: The percent of discard seed; calculated as the sum of discarded tip kernels and extra-large kernels.

LOCUS: A specific location on a chromosome.

LOCUS CONVERSION (Also called a TRAIT CONVERSION): A locus conversion refers to a modified plant within a variety that retains the overall genetics of the variety and further includes a locus with one or more specific desired traits, and otherwise has the same, essentially the same, all or essentially all of the physiological and morphological characteristics of the variety, such as listed in Table 1. Traits can be directed to, for example, modified grain, male sterility, insect control, disease control, or herbicide tolerance. Traits can be mutant genes, transgenic sequences or native traits. A single locus conversion refers to plants within a variety that have been modified in a manner that retains the overall genetics of the variety and include a single locus with one or more specific desired traits. A single locus conversion can include at least or about 1, 2, 3, 4 or 5 traits and less than or about 15, 10, 9, 8, 7 or 6 traits. A locus converted plant can include, for example, at least or about 1, 2 or 3 and less than or about 20, 15, 10, 9, 8, 7, 6, or 5 modified loci while still retaining the overall genetics of the variety and otherwise having essentially the same, the same, all or essentially all of the physiological and morphological characteristics of the variety, such as listed in Table 1. The total number of traits at one or more locus conversions can be, for example, at least or about 1, 2, 3, 4 or 5 and less than or about 25, 20, 15, 10, 9, 8, 7 or 6. Examples of single locus conversions include mutant genes, transgenes and native traits finely mapped to a single locus. Traits may be introduced into a single corn variety by transformation, backcrossing, or a combination of both.

L/POP=YIELD AT LOW DENSITY: Yield ability at relatively low plant densities on a 1 to 9 relative system with a higher number indicating the hybrid responds well to low plant densities for yield relative to other hybrids. A 1, 5, and 9 would represent very poor, average, and very good yield response, respectively, to low plant density.

LRTLDG=LATE ROOT LODGING: The percentage of plants that do not root lodge after anthesis through harvest; plants that lean from the vertical axis at an approximately 30 degree angle or greater would be counted as root lodged. Data are collected only when sufficient selection pressure exists in the experiment measured.

LRTLPN=LATE ROOT LODGING: An estimate of the percentage of plants that do not root lodge after anthesis through harvest; plants that lean from the vertical axis at an approximately 30 degree angle or greater would be considered as root lodged. Data are collected only when sufficient selection pressure exists in the experiment measured.

LRTLSC=LATE ROOT LODGING SCORE: Score for severity of plants that lean from a vertical axis at an approximate 30 degree angle or greater which typically results from strong winds after flowering. Recorded prior to harvest when a root-lodging event has occurred. This lodging results in plants that are leaned or “lodged” over at the base of the plant and do not straighten or “goose-neck” back to a vertical position. Expressed as a 1 to 9 score with 9 being no lodging. Data are collected only when sufficient selection pressure exists in the experiment measured.

MDMCPX=MAIZE DWARF MOSAIC COMPLEX (MDMV=Maize Dwarf Mosaic Virus and MCDV=Maize Chlorotic Dwarf Virus): A 1 to 9 visual rating indicating the resistance to Maize Dwarf Mosaic Complex. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

MILKLN=percent milk in mature grain.

MST=HARVEST MOISTURE: The moisture is the actual percentage moisture of the grain at harvest.

MSTADV=MOISTURE ADVANTAGE: The moisture advantage of variety #1 over variety #2 as calculated by: MOISTURE of variety #2−MOISTURE of variety #1=MOISTURE ADVANTAGE of variety #1.

NEI DISTANCE: A quantitative measure of percent similarity between two varieties. Nei's distance between varieties A and B can be defined as 1−(2*number alleles in common/(number alleles in A+number alleles in B). For example, if varieties A and B are the same for 95 out of 100 alleles, the Nei distance would be 0.05. If varieties A and B are the same for 98 out of 100 alleles, the Nei distance would be 0.02.

NLFBLT=NORTHERN LEAF BLIGHT (Helminthosporium turcicum or Exserohilum turcicum): A 1 to 9 visual rating indicating the resistance to Northern Leaf Blight. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

OILT=GRAIN OIL: Absolute value of oil content of the kernel as predicted by Near-Infrared Transmittance and expressed as a percent of dry matter.

PERCENT IDENTITY: Percent identity as used herein refers to the comparison of the alleles present in two varieties. For example, when comparing two inbred plants to each other, each inbred plant will have the same allele (and therefore be homozygous) at almost all of their loci. Percent identity is determined by comparing a statistically significant number of the homozygous alleles of two varieties. For example, a percent identity of 90% between PH2DMA and other variety means that the two varieties have the same homozygous alleles at 90% of their loci.

PLANT: As used herein, the term “plant” includes reference to an immature or mature whole plant, including a plant that has been detasseled or from which seed or grain has been removed.

PLANT PART: As used herein, the term “plant part” includes one or more of leaves, stems, roots, root tips, anthers, pollen, ovules, flowers, ears, cobs, husks, stalks, root tips, anthers, pericarp, silk, tissue, plant cells and the like. The plant part comprises the genotype, whether haploid or diploid, of the seed from which it was grown.

PLANT SEED: As used herein, a plant seed includes reference to the seed, grain, endosperm, seed coat, pericarp and embryo.

PLATFORM indicates the variety with the base genetics and the variety with the base genetics comprising locus conversion(s). There can be a platform for the inbred maize variety and the hybrid maize variety.

POLPRD=POLLEN PRODUCTION SCORE: The estimated total amount of pollen produced by tassels based on the number of tassel branches and the density of the spikelets.

POLSC=POLLEN SCORE: A 0 to 9 visual rating indicating the amount of pollen shed. The higher the score the more pollen shed.

POLWT=POLLEN WEIGHT: This is calculated by dry weight of tassels collected as shedding commences minus dry weight from similar tassels harvested after shedding is complete.

POP K/A=PLANT POPULATIONS: Measured as 1000's per acre.

POP ADV=PLANT POPULATION ADVANTAGE: The plant population advantage of variety #1 over variety #2 as calculated by PLANT POPULATION of variety #2−PLANT POPULATION of variety #1=PLANT POPULATION ADVANTAGE of variety #1.

PRM=PREDICTED RELATIVE MATURITY: This trait, predicted relative maturity, is based on the harvest moisture of the grain. The relative maturity rating is based on a known set of checks and utilizes standard linear regression analyses and is also referred to as the Comparative Relative Maturity Rating System that is similar to the Minnesota Relative Maturity Rating System.

PRMSHD: A relative measure of the growing degree units (GDU) required to reach 50% pollen shed. Relative values are predicted values from the linear regression of observed GDU's on relative maturity of commercial checks.

PROT=GRAIN PROTEIN: Absolute value of protein content of the kernel as predicted by Near-Infrared Transmittance and expressed as a percent of dry matter.

RESISTANCE: Synonymous with tolerance. The ability of a plant to withstand exposure to an insect, disease, herbicide or other condition. A resistant plant variety will have a level of resistance higher than a comparable wild-type variety.

RTLDG=ROOT LODGING: Root lodging is the percentage of plants that do not root lodge; plants that lean from the vertical axis at an approximately 30 degree angle or greater would be counted as root lodged. Data are collected only when sufficient selection pressure exists in the experiment measured.

RTLADV=ROOT LODGING ADVANTAGE: The root lodging advantage of variety #1 over variety #2. Data are collected only when sufficient selection pressure exists in the experiment measured.

SCTGRN=SCATTER GRAIN: A 1 to 9 visual rating indicating the amount of scatter grain (lack of pollination or kernel abortion) on the ear. The higher the score the less scatter grain.

SDGVGR=SEEDLING VIGOR: This is the visual rating (1 to 9) of the amount of vegetative growth after emergence at the seedling stage (approximately five leaves). A higher score indicates better vigor.

SEED: Fertilized and ripened ovule, consisting of the plant embryo, varying amounts of stored food material, and a protective outer seed coat. Synonymous with grain.

SEFIELD: Percent stress emergence in field.

SELAB: Average % stress emergence in lab tests.

SEL IND=SELECTION INDEX: The selection index gives a single measure of the hybrid's worth based on information for multiple traits. A maize breeder may utilize his or her own set of traits for the selection index. One of the traits that is almost always included is yield. The selection index data presented in the tables represent the mean value averaged across testing stations.

SELF POLLINATION: A plant is self-pollinated if pollen from one flower is transferred to the same or another flower of the same plant.

SIB POLLINATION: A plant is sib-pollinated when individuals within the same family or variety are used for pollination.

SLFBLT=SOUTHERN LEAF BLIGHT (Helminthosporium maydis or Bipolaris maydis): A 1 to 9 visual rating indicating the resistance to Southern Leaf Blight. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

SOURST=SOUTHERN RUST (Puccinia polysora): A 1 to 9 visual rating indicating the resistance to Southern Rust. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

STAGRN=STAY GREEN: Stay green is the measure of plant health near the time of black layer formation (physiological maturity). A high score indicates better late-season plant health.

STDADV=STALK STANDING ADVANTAGE: The advantage of variety #1 over variety #2 for the trait STKCNT.

STKCNT=NUMBER OF PLANTS: This is the final stand or number of plants per plot.

STKCTE: This is the early stand count of plants per plot.

STKLDG=STALK LODGING REGULAR: This is the percentage of plants that did not stalk lodge (stalk breakage) at regular harvest (when grain moisture is between about 20% and 30%) as measured by either natural lodging or pushing the stalks and determining the percentage of plants that break below the ear. Data are collected only when sufficient selection pressure exists in the experiment measured.

STKLDS=STALK LODGING SCORE: A plant is considered as stalk lodged if the stalk is broken or crimped between the ear and the ground. This can be caused by any or a combination of the following: strong winds late in the season, disease pressure within the stalks, ECB damage or genetically weak stalks. This trait should be taken just prior to or at harvest. Expressed on a 1 to 9 scale with 9 being no lodging. Data are collected only when sufficient selection pressure exists in the experiment measured.

STLLPN=LATE STALK LODGING: This is the percent of plants that did not stalk lodge (stalk breakage or crimping) at or around late season harvest (when grain moisture is below 20%) as measured by either natural lodging or pushing the stalks and determining the percentage of plants that break or crimp below the ear. Data are collected only when sufficient selection pressure exists in the experiment measured.

STLPCN=STALK LODGING REGULAR: This is an estimate of the percentage of plants that did not stalk lodge (stalk breakage) at regular harvest (when grain moisture is between about 20% and 30%) as measured by either natural lodging or pushing the stalks and determining the percentage of plants that break below the ear. Data are collected only when sufficient selection pressure exists in the experiment measured.

STLTIP=STERILE TIPS SCORE: The visual 1 to 9 rating of the relative lack of glumes on the tassel central spike and branches. A higher score indicates a lower incidence of sterile tips or lack of glumes on the tassel.

STRT=GRAIN STARCH: Absolute value of starch content of the kernel as predicted by Near-Infrared Transmittance and expressed as a percent of dry matter.

STWWLT=Stewart's Wilt (Erwinia stewartii): A 1 to 9 visual rating indicating the resistance to Stewart's Wilt. A higher score indicates a higher resistance. Data are collected only when sufficient selection pressure exists in the experiment measured.

SSRs: Genetic markers based on polymorphisms in repeated nucleotide sequences, such as microsatellites. A marker system based on SSRs can be highly informative in linkage analysis relative to other marker systems in that multiple alleles may be present.

TASBLS=TASSEL BLAST: A 1 to 9 visual rating was used to measure the degree of blasting (necrosis due to heat stress) of the tassel at the time of flowering. A 1 would indicate a very high level of blasting at time of flowering, while a 9 would have no tassel blasting. Data are collected only when sufficient selection pressure exists in the experiment measured.

TAS WT=TASSEL WEIGHT: This is the average weight of a tassel (grams) just prior to pollen shed.

TILLER=TILLERS: A count of the number of tillers per plot that could possibly shed pollen was taken. Data are given as a percentage of tillers: number of tillers per plot divided by number of plants per plot. A tiller is defined as a secondary shoot that has developed as a tassel capable of shedding pollen.

TSTWTN=TEST WEIGHT (ADJUSTED): The measure of the weight of the grain (in pounds) for a given volume (bushel), adjusted for MST less than or equal to 22%.

TSTWTN=TEST WEIGHT (UNADJUSTED): The measure of the weight of the grain in pounds for a given volume (bushel).

TSWADV=TEST WEIGHT ADVANTAGE: The test weight advantage of variety #1 over variety #2.

VARIETY: A maize line and minor genetic modifications thereof that retain the overall genetics of the line including but not limited to a locus conversion, a mutation, or a somoclonal variant.

WIN M %=PERCENT MOISTURE WINS.

WIN Y %=PERCENT YIELD WINS.

YIELD BU/A=YIELD (BUSHELS/ACRE): Yield of the grain at harvest by weight or volume (bushels) per unit area (acre) adjusted to 15% moisture.

YLDADV=YIELD ADVANTAGE: The yield advantage of variety #1 over variety #2 as calculated by: YIELD of variety #1−YIELD variety #2=YIELD ADVANTAGE of variety #1.

YIELDMST=YIELD/MOISTURE RATIO.

YLDSC=YIELD SCORE: A 1 to 9 visual rating was used to give a relative rating for yield based on plot ear piles. The higher the rating the greater visual yield appearance.

DETAILED DESCRIPTION

All tables discussed herein are provided at the end of this section.

Breeding History of PH2DMA

Inbred maize variety PH2DMA was developed by the following method. Pioneer variety PH2DMA, an inbred of Yellow corn (Zea mays L.), was developed by Pioneer Hi-Bred International, Inc. from a cross made in 2007 in Pessina Cremonese, IT between PHW0V, which was disclosed in PVP Certificate No. 200800263, and a proprietary inbred using the pedigree method of plant breeding.

Maize variety PH2DMA, being substantially homozygous, can be reproduced by planting seeds of the variety, growing the resulting maize plants under self-pollinating or sib-pollinating conditions with adequate isolation, and harvesting the resulting seed using techniques familiar to the agricultural arts.

Phenotypic Characteristics of PH2DMA

Inbred maize variety PH2DMA may be used as a male or female in the production of the first generation F1 hybrid. Inbred maize variety PH2DMA has a relative maturity of approximately 117 based on the Comparative Relative Maturity Rating System for harvest moisture of grain. The variety has shown uniformity and stability within the limits of environmental influence for all the traits as described in the Variety Description Information (Table 1, found at the end of the section). The variety has been self-pollinated and ear-rowed a sufficient number of generations with careful attention paid to uniformity of plant type to ensure the homozygosity and phenotypic stability necessary for use in commercial hybrid seed production. The variety has been increased both by hand and in isolated fields with continued observation for uniformity. No variant traits have been observed or are expected in PH2DMA.

Genotypic Characteristics of PH2DMA

In addition to phenotypic observations, a plant can also be identified by its genotype. The genotype of a plant can be characterized through a genetic marker profile.

As a result of inbreeding, PH2DMA is substantially homozygous. This homozygosity can be characterized at the loci shown in a marker profile. An F1 hybrid made with PH2DMA would substantially comprise the marker profile of PH2DMA. This is because an F1 hybrid is the sum of its inbred parents, e.g., if one inbred parent is homozygous for allele x at a particular locus, and the other inbred parent is homozygous for allele y at that locus, the F1 hybrid will be xy (heterozygous) at that locus. A genetic marker profile can therefore be used to identify hybrids comprising PH2DMA as a parent, since such hybrids will comprise two sets of alleles, one set of which will be from PH2DMA. The determination of the male set of alleles and the female set of alleles may be made by profiling the hybrid and the pericarp of the hybrid seed, which is composed of maternal parent cells. One way to obtain the paternal parent profile is to subtract the pericarp profile from the hybrid profile.

Subsequent generations of progeny produced by selection and breeding are expected to be of genotype xx (homozygous), yy (homozygous), or xy (heterozygous) for these locus positions. When the F1 plant is used to produce an inbred, the resulting inbred should be either x or y for that allele.

Therefore, in accordance with the above, disclosed is a PH2DMA progeny maize plant, seed or plant part that is a first generation (F1) hybrid maize plant comprising two sets of alleles, wherein one set of the alleles is the same as PH2DMA at substantially all loci. A maize cell wherein one set of the alleles is the same as PH2DMA at substantially all loci is also disclosed. The maize cell may be a part of a hybrid seed, plant or plant part produced by crossing PH2DMA with another maize plant. The maize cell may be a somatic cell.

Genetic marker profiles can be obtained by techniques such as Restriction Fragment Length Polymorphisms (RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs), Arbitrarily Primed Polymerase Chain Reaction (AP-PCR), DNA Amplification Fingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs), Amplified Fragment Length Polymorphisms (AFLPs), Simple Sequence Repeats (SSRs) which are also referred to as Microsatellites, and Single Nucleotide Polymorphisms (SNPs).

Any type of marker or marker profile can be used which provides a means of distinguishing varieties. In addition to being used for identification of maize variety PH2DMA, a hybrid produced through the use of PH2DMA, and the identification or verification of pedigree for progeny plants produced through the use of PH2DMA, a genetic marker profile is also useful in developing a locus conversion of PH2DMA.

PH2DMA and its plant parts and seeds can be identified through a molecular marker profile. Such plant parts may be either diploid or haploid. Also encompassed are plants, seeds and plant parts substantially benefiting from the use of PH2DMA in their development, such as PH2DMA comprising a locus conversion.

Comparing PH2DMA to Other Inbreds

A breeder uses various methods to help determine which plants should be selected from segregating populations and ultimately which inbred varieties will be used to develop hybrids for commercialization. In addition to knowledge of the germplasm and plant genetics, a part of the selection process is dependent on experimental design coupled with the use of statistical analysis, which help determine which plants, plant families, inbred varieties and hybrid combinations are significantly better or different for one or more traits of interest. Experimental design methods can be used to assess error so that differences between two inbred varieties or two hybrid varieties can be more accurately evaluated. Trait values can be measured on plants grown under the same or substantially similar environmental conditions appropriate for the traits or traits being evaluated. For example, a locus conversion of PH2DMA for a trait such as herbicide tolerance can be compared with an isogenic counterpart in the absence of the converted trait.

Development of Maize Hybrids Using PH2DMA

A single cross maize hybrid results from the cross of two inbred varieties, each of which has a genotype that complements the genotype of the other. A hybrid progeny of the first generation is designated F1. Hybrid vigor, or heterosis, can be manifested in many polygenic traits, including increased vegetative growth and increased yield.

PH2DMA may be used to produce hybrid maize. In certain embodiments, the methods of crossing maize variety PH2DMA with another maize plant, such as a different maize variety are provided, to form a first generation F1 hybrid seed. The F1 hybrid seed, plant and plant part produced by this method are provided. The first generation F1 seed, plant and plant part will comprise an essentially complete set of the alleles of variety PH2DMA. In some embodiments, methods to identify a particular F1 hybrid plant produced using variety PH2DMA are provided. F1 hybrids with transgenic, male sterile and/or locus conversions of variety PH2DMA are also provided.

PH2DMA may be used to produce a single cross hybrid, a double cross hybrid, or a three-way hybrid. A single cross hybrid is produced when two inbred varieties are crossed to produce the F1 progeny. A double cross hybrid is produced from four inbred varieties crossed in pairs (A×B and C×D) and then the two F1 hybrids are crossed again (A×B)×(C×D). A three-way cross hybrid is produced from three inbred varieties where two of the inbred varieties are crossed (A×B) and then the resulting F1 hybrid is crossed with the third inbred (A×B)×C. In each case, pericarp tissue from the female parent will be a part of and protect the hybrid seed.

Data, such as molecular marker profiles, from PH2DMA may be generated and used in a plant breeding process. For example, nucleic acids may be isolated from a seed of PH2DMA or from a plant, plant part, seed or cell produced by growing a seed of PH2DMA, or from a seed of PH2DMA with a locus conversion, or from a plant, plant part, or cell of PH2DMA with a locus conversion and data may be collected or recorded based on the nucleic acids. One or more polymorphisms may be isolated or identified from the nucleic acids. A plant having one or more of the identified polymorphisms may be selected and used in a plant breeding method to produce another plant.

Combining Ability of PH2DMA

Combining ability of a variety, as well as the performance of the variety per se, is a factor in the selection of improved maize inbreds. Combining ability refers to a variety's contribution as a parent when crossed with other varieties to form hybrids. The hybrids formed for the purpose of selecting superior varieties may be referred to as test crosses, and include comparisons to other hybrid varieties grown in the same environment (same cross, location and time of planting). One way of measuring combining ability is by using values based in part on the overall mean of a number of test crosses weighted by number of experiment and location combinations in which the hybrid combinations occurs. The mean may be adjusted to remove environmental effects and known genetic relationships among the varieties.

General combining ability provides an overall score for the inbred over a large number of test crosses. Specific combining ability provides information on hybrid combinations formed by PH2DMA and a specific inbred parent. A variety such as PH2DMA which exhibits good general combining ability may be used in a large number of hybrid combinations.

A general combining ability report for PH2DMA is provided in Table 2. In Table 2, found at the end of this section, BLUP, Best Linear Unbiased Prediction, values are reported for the breeding value of the maize inbred PH2DMA platform. The BLUP values are reported for numerous traits of hybrids that have inbred PH2DMA or a locus conversion of PH2DMA as a parent. The inbred PH2DMA and various locus conversions of PH2DMA are together considered a platform. The values reported indicate a BLUP value averaged for all members of the platform weighted by the inverse of the Standard Errors.

Hybrid Comparisons

Hybrid comparisons are disclosed which represent specific hybrid crosses from PH2DMA compared with other hybrids with favorable characteristics. Comparisons can illustrate the good specific combining ability of PH2DMA.

The results in Table 3 compare a specific hybrid for which PH2DMA is a parent with other hybrids. The data in Table 3 show that one or more species of the genus of F1 hybrids created with PH2DMA have been reduced to practice. These data illustrate the good specific combining ability of PH2DMA. In Table 3, found at the end of this section, BLUP values are reported for different hybrids wherein one parent is the maize variety PH2DMA or PH2DMA comprising locus conversions. The BLUP values and Standard Errors, SE, are reported for numerous traits. The data presented for these hybrids is based on replicated field trials.

Locus Conversions of PH2DMA

PH2DMA represents a base genetic variety into which a new locus may be introgressed. Direct transformation and backcrossing represent two methods that can be used to accomplish such an introgression. The term locus conversion is used to designate the product of such an introgression.

A locus conversion of PH2DMA will retain the genetic integrity of PH2DMA. and include a locus conversion, which can be determined, for example, using SSR or SNP markers. For example, a locus conversion of PH2DMA can be developed by introducing naturally occurring or transgenic DNA sequences through backcrossing, with PH2DMA utilized as the recurrent parent. At least 1, 2, 3, 5, 5, 6, 7, 8 or 9 or more backcrosses can be used. Molecular marker assisted breeding or selection may be utilized to reduce the number of backcrosses necessary to achieve the backcross conversion.

The complexity of the backcross conversion method depends on the type of trait being transferred. For example, single or closely linked genes may be more straightforward than unlinked genes. Backcrossing can be carried out with high or low expression of the trait, and with cytoplasmic or nuclear inheritance. Desired traits that may be transferred through locus conversion include, but are not limited to, waxy starch, sterility (nuclear and cytoplasmic), fertility restoration, grain color (white), nutritional enhancements, drought resistance, enhanced nitrogen utilization efficiency, altered nitrogen responsiveness, altered fatty acid profile, increased digestibility, low phytate, industrial enhancements, disease resistance (bacterial, fungal or viral), insect resistance, herbicide tolerance and yield enhancements. A locus conversion, also called a trait conversion, can be a native trait or a transgenic trait. In addition, an introgression site itself, such as an FRT site, Lox site or other site specific integration site, may be inserted by backcrossing and utilized for direct insertion of one or more genes of interest into a specific plant variety. The seed industry commonly markets “triple stacks” of base genetics; which can be varieties comprising a locus conversion of at least 3 loci. Similarly, “quadruple stacks” can comprise a locus conversion of at least 4 loci. A single locus may contain several transgenes, such as a transgene for disease resistance and herbicide tolerance in the same expression cassette. Herbicide tolerance may be used as a selectable marker and/or as a phenotypic trait. A locus conversion of a site specific integration system allows for the integration of multiple genes at the converted loci. SSI and FRT technologies may result in multiple gene introgressions at a single locus.

The locus conversion may include, for example, the transfer of a dominant or recessive allele. Selection of progeny containing the trait of interest is accomplished by direct selection for a trait associated with a dominant allele. Transgenes transferred via backcrossing may function as a dominant single gene trait or a recessive allele. Recessive traits may require additional progeny testing in successive backcross generations to determine the presence of the locus of interest. The last backcross generation is usually selfed to give pure breeding progeny for the gene(s) being transferred, although a backcross conversion with a stably introgressed trait may also be maintained by further backcrossing to the recurrent parent with selection for the converted trait.

Along with selection for the trait of interest, progeny can be selected for the phenotype and/or genotype of the recurrent parent. When one or more traits are introgressed into the variety, a difference in quantitative agronomic traits, such as yield or dry down between the variety and an introgressed version of the variety in some environments may occur. For example, the introgressed version may provide a net yield increase in environments where the trait provides a benefit, such as when a variety with an introgressed trait for insect resistance is grown in an environment where insect pressure exists, or when a variety with herbicide tolerance is grown in an environment where herbicide is used.

One process for adding or modifying a trait or locus in maize variety PH2DMA comprises crossing PH2DMA plants grown from PH2DMA seed with plants of another maize variety that comprise the desired trait or locus, selecting F1 progeny plants that comprise the desired trait or locus to produce selected F1 progeny plants, crossing the selected progeny plants with the PH2DMA plants to produce backcross progeny plants, selecting for backcross progeny plants that have the desired trait or locus and the phenotypic characteristics of maize variety PH2DMA to produce selected backcross progeny plants; and backcrossing to PH2DMA one or more times in succession to produce backcross progeny plants that comprise said trait or locus. The modified PH2DMA may be further characterized as having essentially the same phenotypic characteristics of maize variety PH2DMA listed in Table 1 and/or may be characterized by percent identity to PH2DMA as determined by molecular markers, such as SSR markers or SNP markers.

In addition, the above process and other similar processes described herein may be used to produce F1 hybrid maize seed by adding a step at the end of the process that comprises crossing PH2DMA with the locus conversion with a different maize plant and harvesting the resultant F1 hybrid maize seed.

Traits are also used by those of ordinary skill in the art to characterize progeny. Traits are commonly evaluated at a significance level, such as a 1%, 5% or 10% significance level, when measured in plants grown in the same environmental conditions.

Male Sterility and Hybrid Seed Production

Hybrid seed production requires elimination or inactivation of pollen produced by the female inbred parent. Incomplete removal or inactivation of the pollen provides the potential for self-pollination. A reliable method of controlling male fertility in plants offers the opportunity for improved seed production.

PH2DMA can be produced in a male-sterile form. There are several ways in which a maize plant can be manipulated so that it is male sterile. These include use of manual or mechanical emasculation (or detasseling), use of one or more genetic factors that confer male sterility, including cytoplasmic genetic and/or nuclear genetic male sterility, use of gametocides and the like. A male sterile designated PH2DMA may include one or more genetic factors, which result in cytoplasmic genetic and/or nuclear genetic male sterility. All of such embodiments are within the scope of the present claims. The male sterility may be either partial or complete male sterility.

Hybrid maize seed is often produced by a male sterility system incorporating manual or mechanical detasseling. Alternate strips of two maize inbreds are planted in a field, and the pollen-bearing tassels are removed from one of the inbreds (female). Provided that there is sufficient isolation from sources of foreign maize pollen, the ears of the detasseled inbred will be fertilized only from the other inbred (male), and the resulting seed is therefore hybrid and will form hybrid plants.

The laborious detasseling process can be avoided by using cytoplasmic male-sterile (CMS) inbreds. Plants of a CMS inbred are male sterile as a result of genetic factors in the cytoplasm, as opposed to the nucleus, and so nuclear linked genes are not transferred during backcrossing. Thus, this characteristic is inherited exclusively through the female parent in maize plants, since only the female provides cytoplasm to the fertilized seed. CMS plants are fertilized with pollen from another inbred that is not male-sterile. Pollen from the second inbred may or may not contribute genes that make the hybrid plants male-fertile, and either option may be preferred depending on the intended use of the hybrid. The same hybrid seed, a portion produced from detasseled fertile maize and a portion produced using the CMS system, can be blended to insure that adequate pollen loads are available for fertilization when the hybrid plants are grown.

There are several methods of conferring genetic male sterility available, such as providing multiple mutant genes at separate locations within the genome that confer male sterility, chromosomal translocations, and nuclear male sterility by identifying a gene needed for male fertility; silencing this gene and removing and replacing its native promoter with an inducible promoter; and inserting this genetically engineered gene back into the plant. Fertility can be restored by inducing, or turning “on”, the promoter, which in turn allows the gene that confers male fertility to be transcribed. See U.S. Pat. Nos. 3,861,709, 3,710,511, 4,654,465, 4,727,219 and 5,432,068, the entire disclosures of each of which are herein incorporated by reference.

Other methods include delivering into the plant a gene encoding a cytotoxic substance associated with a male tissue specific promoter or an antisense system in which a fertility gene is identified and an antisense to that gene is inserted in the plant (see International Patent Publication WO 90/08828). Other methods make use of gametocides which are chemicals affect cells needed for male fertility only for the growing season in which the gametocide is applied. Incomplete control over male fertility may result in self-pollinated seed being unintentionally harvested and packaged with hybrid seed. Once the seed from the hybrid bag is planted, it is possible to identify and select these self-pollinated plants though phenotypic observation or molecular marker analyses.

Transformation

Provided are methods of transformation, transformed versions of maize variety PH2DMA, as well as hybrid combinations thereof. Transformed or transgenic plants may contain and express foreign genetic elements, or additional, or modified versions of native or endogenous genetic elements. Any DNA sequences, whether from a different species or from the same species, which are stably inserted into the cell using transformation are referred to herein collectively as “transgenes” and/or “transgenic events”. In some embodiments, a transformed variant of PH2DMA may comprise at least one transgene but may contain at least about or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 transgenes and less than about or about 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, 3, or 2 transgenes.

Numerous methods for plant transformation have been developed, including biological and physical plant transformation protocols. In addition, expression vectors and in vitro culture methods for plant cell or tissue transformation and regeneration of plants are available. In some embodiments, plant transformation involves the use or construction of an expression vector. Such a vector may comprise a DNA sequence that contains a gene under the control of or operatively linked to a regulatory element, for example a promoter. The vector may contain one or more genes and one or more regulatory elements. Regulatory constructs which up regulate or down regulate a gene of interest may also be used.

A transgenic event which has been stably engineered into the germ cell line of a particular maize plant using transformation techniques, can be moved into the germ cell line of another variety using traditional breeding techniques that are well known in the plant breeding arts. For example, a backcrossing may be used to move a transgenic event from a transformed maize plant to another variety, such that the resulting progeny comprise the transgenic event(s). If an inbred variety is used for the transformation, then the transgenic inbred plants can be crossed to a different inbred in order to produce a transgenic hybrid maize plant.

Various genetic elements can be introduced into the plant genome using transformation. These elements include, but are not limited to genes; coding sequences; inducible, constitutive, and tissue specific promoters; enhancing sequences; and signal and targeting sequences. For example, see the traits, genes and transformation methods listed in U.S. Pat. Nos. 6,118,055 and 6,284,953, which are herein incorporated by reference. In addition, transformability of a variety can be increased by introgressing the trait of high transformability from another variety known to have high transformability, such as Hi-II. See U.S. Patent Application Publication US2004/0016030, incorporated herein by reference in its entirety. In some embodiments, methods for mapping transgenic events are provided.

In some embodiments, a foreign protein can be produced in commercial quantities using transgenic plants described herein. The transgenic plants can be harvested in a conventional manner and a foreign protein extracted from a tissue of interest or from total biomass.

In some embodiments, plants are genetically engineered to express various phenotypes of agronomic interest. By altering expression of one or more genes, disease resistance, insect resistance, herbicide tolerance, agronomic traits, grain quality and other traits may be enhanced. Transformation can also be used to insert DNA sequences which control or help control male-sterility. DNA sequences native to maize as well as non-native DNA sequences can be transformed into maize and used to alter levels of native or non-native proteins. Various promoters, targeting sequences, enhancing sequences, and other DNA sequences can be inserted into the maize genome for the purpose of altering the expression of proteins. Reduction of the activity of specific genes (also known as gene silencing, or gene suppression) is desirable for several aspects of genetic engineering in plants.

In some embodiments, the plants may be transformed by reducing expression of a gene, including for example one of more of the use of knock-outs, or other genetic elements such as a FRT, Lox or other site specific integration site, antisense technology, co-suppression, RNA interference, virus-induced gene silencing, target-RNA-specific ribozymes, microRNA and amiRNA, Zn-finger targeted molecules; and other methods or combinations thereof.

Exemplary nucleotide sequences that may be altered by genetic engineering include, but are not limited to, those categorized below.

1. Transgenes that Confer Resistance to Insects or Disease and that Encode:

(A) Plant disease resistance genes. A plant resistant to a disease is one that is more resistant to a pathogen as compared to the wild type plant.

(B) A Bacillus thuringiensis protein, a derivative thereof or a synthetic polypeptide modeled thereon. See, for example, U.S. Pat. Nos. 5,188,960, 5,689,052, 5,880,275, 5,986,177, 7,105,332, 7,208,474, 7,449,552, 7,468,278, 7,510,878, 7,521,235, 7,605,304, 7,629,504, 7,329,736, 7,696,412, 7,772,465, 7,790,846, 7,858,849 and 7,858,849 and International Publication Nos. WO 91/14778; WO 99/31248; WO 01/12731; WO 99/24581; and WO 97/40162, the entire disclosures of which are herein incorporated by reference.

(C) An insect-specific hormone or pheromone such as an ecdysteroid and juvenile hormone, a variant thereof, a mimetic based thereon, or an antagonist or agonist thereof.

(D) An insect-specific peptide which, upon expression, disrupts the physiology of the affected pest.

(E) An enzyme responsible for a hyperaccumulation of a monoterpene, a sesquiterpene, a steroid, hydroxamic acid, a phenylpropanoid derivative or another non-protein molecule with insecticidal activity.

(F) An enzyme involved in the modification, including the post-translational modification, of a biologically active molecule; for example, a glycolytic enzyme, a proteolytic enzyme, a lipolytic enzyme, a nuclease, a cyclase, a transaminase, an esterase, a hydrolase, a phosphatase, a kinase, a phosphorylase, a polymerase, an elastase, a chitinase and a glucanase, whether natural or synthetic. See, for example, U.S. Pat. Nos. 6,563,020; 7,145,060 and 7,087,810, the entire disclosures of which are herein incorporated by reference. Examples include, without limitation, a callase gene, a chitinase-encoding sequence such as tobacco hookworm chitinase, and a ubi4-2 polyubiquitin gene.

(G) A molecule that stimulates signal transduction, for example, a calmodulin encoding sequence.

(H) A hydrophobic moment peptide. See, for example, PCT application Publications WO 95/16776 and WO 95/18855 and U.S. Pat. Nos. 5,607,914 and 5,580,852, the disclosures of which are herein incorporated by reference in their entireties.

(I) A membrane permease, a channel former or a channel blocker.

(J) A viral-invasive protein or a complex toxin derived therefrom. For example, the accumulation of viral coat proteins in transformed plant cells imparts resistance to viral infection and/or disease development effected by the virus from which the coat protein gene is derived, as well as by related viruses, such as alfalfa mosaic virus, cucumber mosaic virus, tobacco streak virus, potato virus X, potato virus Y, tobacco etch virus, tobacco rattle virus and tobacco mosaic virus.

(K) An insect-specific antibody or an immunotoxin derived therefrom.

(L) A virus-specific antibody.

(M) A developmental-arrestive protein produced in nature by a pathogen or a parasite. For example, fungal endo alpha-1,4-D-polygalacturonases facilitate fungal colonization and plant nutrient release by solubilizing plant cell wall homo-alpha-1,4-D-galacturonase.

(N) A developmental-arrestive protein produced in nature by a plant. For example, a ribosome-inactivating gene may provide resistance to fungal disease.

(O) Genes involved in the Systemic Acquired Resistance (SAR) Response and/or the pathogenesis related genes.

(P) Antifungal genes See, for example, U.S. Pat. Nos. 6,875,907, 6,891,085 and 7,306,946, 7,498,413, 7,589,176, 7,598,3468, and 8,084,671, the disclosures of which are herein incorporated by reference in their entireties.

(Q) Detoxification genes, such as for fumonisin, beauvericin, moniliformin and zearalenone and their structurally related derivatives. For example, see U.S. Pat. Nos. 5,716,820; 5,792,931; 5,798,255; 5,846,812; 6,083,736; 6,538,177; 6,388,171 and 6,812,380, the disclosures of which are herein incorporated by reference in their entireties.

(R) Cystatin and cysteine proteinase inhibitors. See U.S. Pat. No. 7,205,453, the disclosures of which are herein incorporated by reference in their entireties.

(S) Defensin genes. See WO03000863 and U.S. Pat. Nos. 6,911,577; 6,855,865; 6,777,592 and 7,238,781, the disclosures of which are herein incorporated by reference in their entireties.

(T) Genes conferring resistance to nematodes. See e.g. PCT Application WO96/30517; WO93/19181, WO 03/033651 and U.S. Pat. Nos. 6,284,948 and 7,301,069, the disclosures of which are herein incorporated by reference in their entireties.

(U) Genes that confer resistance to Phytophthora Root Rot, such as the Rps 1, Rps 1-a, Rps 1-b, Rps 1-c, Rps 1-d, Rps 1-e, Rps 1-k, Rps 2, Rps 3-a, Rps 3-b, Rps 3-c, Rps 4, Rps 5, Rps 6, Rps 7 and other Rps genes.

(V) Genes that confer resistance to Brown Stem Rot, such as described in U.S. Pat. No. 5,689,035 and incorporated by reference for this purpose.

(W) Genes that confer resistance to Colletotrichum, such as the Rcg locus that may be utilized, for example, as a single locus conversion.

2. Transgenes that Confer Tolerance to a Herbicide, for Example:

(A) A herbicide that inhibits the growing point or meristem, such as an imidazolinone or a sulfonylurea. Exemplary genes in this category code for mutant ALS and AHAS enzyme as described, for example, U.S. Pat. Nos. 5,605,011; 5,013,659; 5,141,870; 5,767,361; 5,731,180; 5,304,732; 4,761,373; 5,331,107; 5,928,937; 5,378,824 and 7,838,263; and international publication WO 96/33270, the disclosures of which are herein incorporated by reference in their entireties.

(B) Glyphosate tolerance may be imparted by mutant 5-enolpyruvl-3-phosphikimate synthase (EPSP) and aroA genes and other phosphono compounds such as glufosinate (phosphinothricin acetyl transferase (PAT) and Streptomyces hygroscopicus phosphinothricin acetyl transferase (bar) genes), pyridinoxy or phenoxy proprionic acids and cyclohexones (ACCase inhibitor-encoding genes), glyphosate oxido-reductases, and glyphosate N-acetyltransferases. See, for example, U.S. Pat. Nos. 4,769,061, 4,940,835, 5,463,175, 5,627,061, 5,776,760, 6,566,587; 6,338,961; 6,248,876; 6,040,497; 7,462,481; 7,405,074, 5,804,425; 5,633,435; 5,145,783; 4,971,908; 5,312,910; 5,188,642; 4,940,835; 5,866,775; 6,225,114 B1; 6,130,366; 5,310,667; 4,535,060; 4,769,061; 5,633,448; 5,510,471; RE. 36,449; RE 37,287; and 5,491,288; U.S. Patent Publication No. 2008-0234130, and International Patent Publication WO 01/66704, each of which are incorporated herein by reference in their entireties for this purpose. Nucleotide sequences of glutamine synthetase genes which confer tolerance to herbicides such as L-phosphinothricin may also be used, see for example, U.S. Pat. Nos. 4,975,374, 5,969,213; 5,489,520; 5,550,318; 5,874,265; 5,919,675; 5,561,236; 5,648,477; 5,646,024; 6,177,616; and 5,879,903, which are incorporated herein by reference in their entireties for this purpose. Exemplary genes conferring resistance to phenoxy proprionic acids and cyclohexones, such as sethoxydim and haloxyfop, are the Acc1-S1, Acc1-S2 and Acc1-S3 genes.

(C) A herbicide that inhibits photosynthesis, such as a triazine (psbA and gs+ genes) and a benzonitrile (nitrilase gene).

(D) Multiple herbicide resistance genes include those encoding an acetohydroxy acid synthase, a chimeric protein of rat cytochrome P4507A1 and yeast NADPH-cytochrome P450 oxidoreductase, glutathione reductase and superoxide dismutase, and genes for various phosphotransferases.

(E) Protoporphyrinogen oxidase (protox) used in the production of chlorophyll, serves as the target for a variety of herbicidal compounds. Plants having altered protox activity and tolerant to these herbicides are described in U.S. Pat. Nos. 6,288,306, 6,282,837, and 5,767,373; and International Patent Publication WO 01/12825, the disclosures of which are herein incorporated by reference in their entireties.

3. Transgenes that Confer or Contribute to an Altered Grain Characteristic, Such as:

(A) Altered fatty acids, for example, by:

-   -   (1) Down-regulation of stearoyl-ACP desaturase to increase         stearic acid content of the plant. See for example WO99/64579,         incorporated herein by reference.     -   (2) Elevating oleic acid via FAD-2 gene modification and/or         decreasing linolenic acid via FAD-3 gene modification. See U.S.         Pat. Nos. 6,063,947; 6,323,392; 6,372,965 and International         Patent Publication No. WO 93/11245, the disclosures of which are         herein incorporated by reference in their entireties.     -   (3) Altering conjugated linolenic or linoleic acid content, such         as in WO 01/12800.     -   (4) Altering LEC1, AGP, Dek1, Superal1, mi1ps, various Ipa genes         such as Ipa1, Ipa3, hpt or hggt. For example, see International         Patent Publications WO 02/42424, WO 98/22604, WO 03/011015,         WO02/057439, WO03/011015, U.S. Pat. Nos. 6,423,886, 6,197,561,         6,825,397, and U.S. Publication Nos. 2003/0079247 and         2003/0204870, the disclosures of which are herein incorporated         by reference in their entireties.

B) Altered phosphorus content, for example, by the:

-   -   (1) Introduction of a phytase-encoding gene would enhance         breakdown of phytate, adding more free phosphate to the         transformed plant.     -   (2) Modulating a gene that reduces phytate content, for example,         altering the LPA alleles or inositol kinase activity. See, for         example, International Patent Publication Nos. WO 05/113778, WO         02/059324, WO 03/027243, WO 99/05298, WO2002/059324, WO         98/45448, WO99/55882, WO01/04147, US Patent Publications         2003/0009011, 2003/0079247, and 2003/0079247, and U.S. Pat. Nos.         6,197,561, 6,291,224, and 6,391,348, the disclosures of which         are herein incorporated by reference in their entireties.

(C) Altered carbohydrates affected, for example, by altering a gene for a fructosyltransferase, a levansucrase, an alpha-amylase, an invertase, a UDP-D-xylose 4-epimerase, an enzyme that affects the branching pattern of starch (such as starch branching enzyme II), a gene altering thioredoxin such as NTR and/or TRX, Fragile 1 and 2, Ref1, HCHL, C4H and/or a gamma zein knock out or mutant such as cs27 or TUSC27 or en27. See U.S. Pat. Nos. 6,531,648, 6,858,778, and 6,232,529; US Patent Publication Nos. 2005/0160488 and 2005/0204418; and International Publication No. WO 99/10498, the disclosures of each of which are incorporated by reference for this purpose.

(D) Altered antioxidant content or composition, such as alteration of tocopherol or tocotrienols, for example, through alteration of a homogentisate geranyl geranyl transferase (hggt). See U.S. Pat. Nos. 6,787,683, and 7,154,029 and International Publication Nos. WO 00/68393 and WO 03/082899, the disclosures of each of which are herein incorporated by reference for this purpose.

(E) Altered essential seed amino acids. For example methionine, lysine, threonine and others, see U.S. Pat. Nos. 5,559,223, 5,633,436, 5,850,016, 5,885,802, 5,885,801, 5,939,599, 5,912,414, 5,990,389, 6,127,600, 6,080,913, 6,346,403, 6,441,274, 6,459,019, 6,664,445, 6,803,498, 6,930,225, 7,179,955, US Patent Publication No. 2004/0068767, and International Publication Nos. WO99/40209, WO99/29882, WO98/20133 WO98/56935, WO98/45458, WO98/42831, WO96/01905, WO95/15392, WO01/79516 the disclosures of each of which are herein incorporated by reference for this purpose.

4. Genes that Control Male-Sterility:

Mutant genes at one or more separate locations within the genome may confer male sterility, such as a deacetylase gene, barnase and barstar genes, and the use of stamen-specific promoters. See U.S. Pat. Nos. 3,861,709, 3,710,511 4,654,465, 4,727,219, 5,432,068, 5,859,341; 6,297,426; 5,478,369; 5,824,524; 5,850,014; and 6,265,640 and International Patent Publication Nos. WO 92/13956, WO 92/13957, and WO 01/29237, the disclosures of each of which are herein incorporated by reference in their entireties.

5. Genes that create a site for site specific DNA integration. For example, the Gin recombinase of phage Mu, the Pin recombinase of E. coli, the R/RS system of the pSR1 plasmid and the introduction of FRT sites used in the FLP/FRT system and/or Lox sites that may be used in the Cre/Loxp system. For example, see WO 99/25821 which is herein incorporated by reference. 6. Genes that affect abiotic stress resistance (including but not limited to flowering, ear and seed development, enhancement of nitrogen utilization efficiency, altered nitrogen responsiveness, drought resistance or tolerance, cold resistance or tolerance, and salt resistance or tolerance) and increased yield under stress. CBF genes and transcription factors may be used to mitigate the negative effects of freezing, high salinity, and drought on plants. Altering abscisic acid, cytokinin or ethylene expression in plants or altering plant transcription factors or transcriptional regulators may increase yield and/or tolerance to abiotic stress. Enhancement of nitrogen utilization and altered nitrogen responsiveness may be exploited. For examples, see U.S. Pat. Nos. 5,892,009; 5,965,705; 5,929,305; 5,891,859; 6,084,153; 6,107,547; 6,177,275, 6,417,428; 6,664,446; 6,706,866; 6,717,034; 6,801,104; 6,992,237; and 7,531,723; International Patent Publication Nos. WO00/73475; WO2000060089; WO2001026459; WO2001035725; WO2001034726; WO2001035727; WO2001036444; WO0164898; WO2001036597; WO2001036598; WO2002015675; WO2002017430; WO200032761; WO2002077185; WO2002079403; WO2003013227; WO2003013228; WO2003014327; WO2004031349; WO2004076638; WO9809521; WO9938977; WO01/36596; WO2000/006341, WO04/090143; WO0202776; and WO2003052063, and U.S. Patent Publication Nos. 20040148654, 20040128719, 20030166197 20040098764 and 20040078852, the disclosures of each of which are herein incorporated by reference in their entireties.

Other genes and transcription factors that affect plant growth and agronomic traits such as yield, flowering, plant growth and/or plant structure, can be introduced or introgressed into plants, see e.g. U.S. Pat. No. 6,573,430 (TFL), 6,713,663 (FT), 6,794,560, and 6,307,126 (GAI), and International Patent Publication Nos. WO97/49811 (LHY), WO98/56918 (ESD4), WO97/10339 WO96/14414 (CON), WO96/38560, WO01/21822 (VRN1), WO00/44918 (VRN2), WO99/49064 (GI), WO00/46358 (FRI), WO97/29123, WO99/09174 (D8 and Rht), WO2004076638 and WO2004031349 (transcription factors), the disclosures of each of which are herein incorporated by reference in their entireties.

Using PH2DMA to Develop Another Maize Plant

Maize varieties such as PH2DMA are typically developed for use in the production of hybrid maize varieties. However, varieties such as PH2DMA also provide a source of breeding material that may be used to develop new maize inbred varieties. Plant breeding techniques known in the art and used in a maize plant breeding program include, but are not limited to, recurrent selection, mass selection, bulk selection, mass selection, backcrossing, pedigree breeding, open pollination breeding, restriction fragment length polymorphism enhanced selection, genetic marker enhanced selection, making double haploids, and transformation. Often combinations of these techniques are used. The development of maize hybrids in a maize plant breeding program requires, in general, the development of homozygous inbred varieties, the crossing of these varieties, and the evaluation (genotypic and/or phenotypic) of the crosses.

Methods for producing a maize plant by crossing a first parent maize plant with a second parent maize plant are provided wherein either the first or second parent maize plant is a maize plant of the variety PH2DMA. The other parent may be any other maize plant, such as another inbred variety or a plant that is part of a synthetic or natural population. Such methods of using the maize variety PH2DMA may include selfing, sibbing, backcrosses, mass selection, pedigree breeding, bulk selection, hybrid production, crosses to populations, and the like. These methods include

In some embodiments, methods are provided for making a homozygous PH2DMA progeny plant substantially similar to PH2DMA by producing or obtaining a seed from the cross of PH2DMA and another maize plant and applying double haploid methods to the F1 seed or F1 plant or to any successive filial generation. Such methods decrease the number of generations required to produce an inbred with similar genetics or characteristics to PH2DMA.

For example, a process of making seed substantially retaining the molecular marker profile of maize variety PH2DMA is contemplated, such process comprising obtaining or producing F1 hybrid seed for which maize variety PH2DMA is a parent, inducing double haploids to create progeny without the occurrence of meiotic segregation, obtaining the molecular marker profile of maize variety PH2DMA, and selecting progeny that retain the molecular marker profile of PH2DMA.

In some embodiments, a maize seed derived from inbred maize variety PH2DMA is produced by crossing a plant or plant part of inbred maize variety PH2DMA with another plant, wherein representative seed of said inbred maize variety PH2DMA has been deposited and wherein said maize seed derived from the inbred maize variety PH2DMA has 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% of the same polymorphisms for molecular markers as the plant or plant part of inbred maize variety PH2DMA. The number of molecular markers used for the molecular marker profile can be the public markers listed in Table 4. The sequences for the public markers listed in Table 4 are publically available in the Panzea database. Molecular markers used in the molecular profile may be, for example, Single Nucleotide Polymorphisms, SNPs. A maize seed derived from inbred maize variety PH2DMA can be produced by crossing a plant or plant part of inbred maize variety PH2DMA with another plant or plant part, wherein representative seed of said inbred maize variety PH2DMA has been deposited and wherein said maize seed derived from the inbred maize variety PH2DMA has all, essentially all, the same, or essentially the same physiological and morphological characteristics as maize variety PH2DMA, such as listed in Table 1, when grown in the same environmental conditions. The same environmental conditions may be, but are not limited to, a side-by-side comparison. The characteristics can be those listed in Table 1. The comparison can be made using any number of professionally accepted experimental designs and statistical analyses.

Use of PH2DMA in Tissue Culture

In some embodiments, the PH2DMA can be used in tissue culture. As used herein, the term “tissue culture” includes plant protoplasts, plant cell tissue culture, cultured microspores, plant calli, plant clumps, and the like. As used herein, phrases such as “growing the seed” or “grown from the seed” include embryo rescue, isolation of cells from seed for use in tissue culture, as well as traditional growing methods.

Tissue culture of maize, including tassel/anther culture, is described in U.S. Patent Publication 20020062506, which is incorporated herein by reference for this purpose. In some aspects, cells are provided which upon growth and differentiation produce maize plants having the genotype and/or phenotypic characteristics of variety PH2DMA.

Seed Treatments and Cleaning

In some embodiments, methods of harvesting the seed of the maize variety PH2DMA as seed for planting are provided. Embodiments may include cleaning the seed, treating the seed, and/or conditioning the seed. Cleaning the seed can encompass removing foreign debris such as weed seed and removing chaff, plant matter, from the seed. Conditioning the seed can include controlling the temperature and rate of dry down and storing seed in a controlled temperature environment. Seed treatment is the application of a composition to the seed such as a coating or powder. Some examples of compositions that can be applied as a seed treatment are insecticides, fungicides, pesticides, antimicrobials, germination inhibitors, germination promoters, cytokinins, and nutrients.

In some embodiments, seed material is treated, typically surface treated, with a composition comprising combinations of chemical or biological herbicides, herbicide safeners, insecticides, fungicides, germination inhibitors and enhancers, nutrients, plant growth regulators and activators, bactericides, nematicides, avicides and/or molluscicides. These compounds can be formulated together with further carriers, surfactants or application-promoting adjuvants customarily employed in the art of formulation. The coatings may be applied by impregnating propagation material with a liquid formulation or by coating with a combined wet or dry formulation. Examples of the various types of compounds that may be used as seed treatments are provided in The Pesticide Manual: A World Compendium, C. D. S. Tomlin Ed., published by the British Crop Production Council, which is hereby incorporated by reference.

Some seed treatments that may be used on crop seed include, but are not limited to, one or more of abscisic acid, acibenzolar-S-methyl, avermectin, amitrol, azaconazole, azospirillum, azadirachtin, azoxystrobin, Bacillus spp. (including one or more of cereus, firmus, megaterium, pumilis, sphaericus, subtilis and/or thuringiensis), Bradyrhizobium spp. (including one or more of betae, canariense, elkanii, iriomotense, japonicum, liaonigense, pachyrhizi and/or yuanmingense), captan, carboxin, chitosan, clothianidin, copper, cyazypyr, difenoconazole, etidiazole, fipronil, fludioxonil, fluoxastrobin, fluquinconazole, flurazole, fluxofenim, harpin protein, imazalil, imidacloprid, ipconazole, isoflavenoids, lipo-chitooligosaccharide, mancozeb, manganese, maneb, mefenoxam, metalaxyl, metconazole, myclobutanil, PCNB, penflufen, penicillium, penthiopyrad, permethrine, picoxystrobin, prothioconazole, pyraclostrobin, rynaxypyr, S-metolachlor, saponin, sedaxane, 2-(thiocyanomethylthio) benzothiazole (TCMTB), tebuconazole, thiabendazole, thiamethoxam, thiocarb, thiram, tolclofos-methyl, triadimenol, trichoderma, trifloxystrobin, triticonazole and/or zinc. PCNB seed coat refers to EPA registration number 00293500419, containing quintozen and terrazole.

INDUSTRIAL APPLICABILITY

In some embodiments, methods of harvesting the grain of the F1 plant of variety PH2DMA and using the grain in a commodity as described herein are provided. Examples of maize grain as a commodity include but are not limited to silage, oils, meals, flour, starches, syrups, proteins, and sugars. Maize grain can be used as human food, livestock feed, to produce ethanol and as raw material in industry. Maize grain may be dry- or wet-milled for consumption or industrial uses. The principal products of maize dry milling are grits, meal and flour. Wet-milling of maize can provide starch, syrups, and dextrose for food use. Maize oil is recovered from maize germ, which is a by-product of both dry- and wet-milling.

Both grain and non-grain portions of the F1 plant may be used as livestock feed, such as for beef cattle, dairy cattle, hogs, and poultry.

Industrial applications of maize starch and flour are based on functional properties, such as viscosity, film formation, adhesive properties, and ability to suspend particles. The maize starch and flour have application in the paper and textile industries. Other industrial uses include applications in adhesives, building materials, foundry binders, laundry starches, explosives, oil-well muds, and other mining applications.

Plant parts may also be used in industry: for example, stalks and husks can be made into paper and wallboard and cobs can be used for fuel and to make charcoal.

TABLE 1 Variety Description Information Current Variety Name PH2DMA Plant height with tassel 250 (cm) Ear height 120 (cm) Leaf width of blade   9 (cm) Leaf limb anthocyanin color intensity of Absent or entire plant Very Weak Number of days to shedding from planting 79 Number of days to silking from planting 81 Bar glume color intensity Absent Nodes anthocyanin color intensity Absent or Very Weak Internode anthocyanin color intensity Absent or Very Weak Length of main axis above highest lateral  18 (cm) branch Length of main axis above lowest lateral  33 (cm) branch Degree of stem zig-zag Absent or very slight Ear husk length Medium Ear shank length scale Short Leaf length score 0.70 m to 0.80 m Ratio height of insertion of peduncle of 0.48 upper ear to plant length Leaf angle between blade and stem Small (6 to 37 degrees) Leaf attitude of entire plant Absent or Very Slight Recurved Leaf tip shape Rounded Foliage intensity of green color Medium Leaf blade undulation of margin Absent or very weak Silk anthocyanin color intensity Absent or Very Weak Anther color Green Anther anthocyanin color intensity Absent or Very Weak Glume color Green Glume anthocyanin coloration at base Absent or Very Weak Glume anthocyanin color excluding base Absent or Very Weak Brace roots anthocyanin coloration Strong Sheath anthocyanin color intensity at first Strong leaf stage Sheath anthocyanin color intensity Absent or very weak Leaf sheath hairiness scale (1-none, 6-fuzzy) 1 Tassel angle between main axis and lateral Small branches Tassel lateral branch curvature Slightly Recurved (6 to 37 degrees) Number of primary lateral tassel branches Very many (>20) Primary tassel branch length Very short Secondary tassel branches (number) 4 to 10 Branches Tassel spikelet density Medium Type of grain Flint Ear shape (taper) Conico cylindrical Ear length 165 (mm) Ear diameter  39 (mm) Number of rows of grain on ear 16 Dorsal side of grain color Orange Top of grain color Orange Kernel shape Cuneiform Cob diameter  21 (mm) Cob color Dark Red Cob anthocyanin Color Intensity Strong Cob glume anthocyanin color intensity Strong

TABLE 2 Inbred PH2DMA platform BLUP breeding values Weighted Trait BLUP value EARHT 48.3 FUSERS 5.5 GDUSHD 129.1 GDUSLK 134.5 MST 23.9 NLFBLT 5.4 PLTHT 111.9 STAGRN 5.4 TSTWT 57.4 TSTWTN 60.3 YIELD 134.7

TABLE 3 Inbred PH2DMA as parent in hybrid EARHT MST PLTHT ftnote BLUP SE BLUP SE BLUP SE Hybrid1 47.2 1.4 24.6 0.3 112.9 1.8 STAGRN TSTWTN YIELD ftnote BLUP SE BLUP SE BLUP SE Hybrid1 5.6 0.4 60.3 0.3 153.4 4.2 a wherein inbred comprises a trait conversion conferring insect control b wherein inbred comprises a trait conversion conferring herbicide tolerance c wherein inbred comprises a trait conversion conferring disease control

TABLE 4 Marker No. Marker Public Name Chromosome Location 1 PHM175.25 1 2 PHM2244.142 1 3 PHM3226.15 1 4 PHM4597.14 1 5 PHM3951.25 1 6 PHM3726.129 1 7 PHM12323.17 1 8 PHM2130.29 1 9 PZA02577.1 1 10 PHM3147.18 1 11 PHM5622.21 1 12 PHM5727.5 1 13 PHM5597.15 1 14 PHM3627.11 1 15 PHM12706.14 1 16 PHM759.24 1 17 PZA00137.2 1 18 PHM3034.3 1 19 PZA00276.18 1 20 PHM673.33 1 21 PHM5817.15 2 22 PHM13440.11 2 23 PHM5535.8 2 24 PZA00396.9 2 25 PHM3334.6 2 26 PHM3309.8 2 27 PZA00200.8 2 28 PHM4425.25 2 29 PHM4586.12 2 30 PZA02058.1 2 31 PHM4780.38 2 32 PHM10404.8 2 33 PHM3457.6 2 34 PHM4620.24 2 35 PZA01537.2 2 36 PHM3055.9 2 37 PZA02731.1 2 38 PHM16125.47 2 39 PHM3668.12 2 40 PZA00163.4 2 41 PZA02266.3 2 42 PHM3094.23 2 43 PHM4259.5 3 44 PHM12859.10 3 45 PHM15475.27 3 46 PHM4145.18 3 47 PHM13823.7 3 48 PHM15474.5 3 49 PHM1745.16 3 50 PHM13420.11 3 51 PHM9914.11 3 52 PHM4621.57 3 53 PHM13673.53 3 54 PZA02122.9 3 55 PZA00892.5 3 56 PHM8828.7 3 57 PHM2672.19 3 58 PZA00817.2 3 59 PZA03013.7 4 60 PHM1971.20 4 61 PHM2438.28 4 62 PHM259.11 4 63 PHM687.25 4 64 PZA03043.14 4 65 PHM5572.19 4 66 PHM13623.14 4 67 PZA00057.2 4 68 PHM9635.30 4 69 PHM3637.14 4 70 PZA00941.2 4 71 PZA01810.2 4 72 PZA01332.2 4 73 PZA00399.10 4 74 PHM5599.20 4 75 PHM5665.10 4 76 PHM2100.21 4 77 PZA00005.5 4 78 PHM5359.10 5 79 PZA02462.1 5 80 PHM3137.17 5 81 PHM9676.10 5 82 PHM3402.11 5 83 PHM6795.4 5 84 PZA00522.7 5 85 PHM1870.20 5 86 PZA02862.10 5 87 PZA02818.10 5 88 PZA02633.4 5 89 PHM3512.186 5 90 PHM4349.3 5 91 PHM2865.8 5 92 PZA02817.15 5 93 PZA03047.12 6 94 PHM12904.7 6 95 PZA00382.17 6 96 PZA02148.1 6 97 PHM5794.13 6 98 PHM4748.16 6 99 PHM1956.90 6 100 PZA01468.1 6 101 PHM4468.13 6 102 PHM9241.13 7 103 PHM4135.15 7 104 PHM3676.33 7 105 PZA00256.27 7 106 PHM4080.15 7 107 PHM4353.31 7 108 PZA00132.17 7 109 PZA00084.2 7 110 PHM5766.12 7 111 PHM9162.135 7 112 PZA00670.2 7 113 PHM1912.20 7 114 PHM5232.11 7 115 PHM5218.14 8 116 PZA02174.2 8 117 PHM4512.38 8 118 PHM2487.6 8 119 PHM5158.13 8 120 PHM1978.111 8 121 PHM2350.17 8 122 PZA01257.1 8 123 PZA00908.2 8 124 PHM934.19 8 125 PHM5805.19 8 126 PHM10525.11 8 127 PHM5468.25 8 128 PHM448.23 8 129 PHM12749.13 8 130 PHM4757.14 8 131 PHM14046.9 8 132 PHM2749.10 8 133 PHM3925.79 9 134 PZA00410.2 9 135 PHM11946.17 9 136 PHM1218.6 9 137 PHM5181.10 9 138 PHM4720.12 9 139 PHM5185.13 9 140 PHM229.15 9 141 PHM13183.12 9 142 PZA00060.2 9 143 PZA02397.12 9 144 PHM816.25 9 145 PHM13681.12 9 146 PHM3631.47 10 147 PHM2828.83 10 148 PHM1752.36 10 149 PZA01451.1 10 150 PHM3922.32 10 151 PHM4066.11 10 152 PZA00562.4 10 153 PHM1155.14 10 154 PZA00400.3 10 155 PHM537.22 10 156 PHM13687.14 10 157 PZA02969.9 10 158 PHM5435.25 10 159 PZA01073.1 10 160 PHM3844.14 10 161 PHM1506.23 10

DEPOSITS

Applicant has made a deposit of at least 2,500 seeds of Maize Variety PH2DMA with the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, Va. 20110-2209, USA, with ATCC Deposit No. PTA-124043. The seeds deposited with the ATCC on Mar. 30, 2017 were are obtained from the seed of the variety maintained by Pioneer Hi-Bred International, Inc., 7250 NW 62^(nd) Avenue, Johnston, Iowa, 50131 since prior to the filing date of this application. Access to this seed will be available during the pendency of the application to the Commissioner of Patents and Trademarks and persons determined by the Commissioner to be entitled thereto upon request. Upon allowance of any claims in the application, the Applicant will make the deposit available to the public pursuant to 37 C.F.R. §1.808. This deposit of the Maize Variety PH2DMA will be maintained in the ATCC depository, which is a public depository, for a period of 30 years, or 5 years after the most recent request, or for the enforceable life of the patent, whichever is longer, and will be replaced if it becomes nonviable during that period. Additionally, Applicant has or will satisfy all of the requirements of 37 C.F.R. §§1.801-1.809, including providing an indication of the viability of the sample upon deposit. Applicant has no authority to waive any restrictions imposed by law on the transfer of biological material or its transportation in commerce. Applicant does not waive any infringement of rights granted under this patent or under the Plant Variety Protection Act (7 USC 2321 et seq.).

The foregoing invention has been described in detail by way of illustration and example for purposes of clarity and understanding. As is readily apparent to one skilled in the art, the foregoing are only some of the methods and compositions that illustrate the embodiments of the foregoing invention. It will be apparent to those of ordinary skill in the art that variations, changes, modifications and alterations may be applied to the compositions and/or methods described herein without departing from the true spirit, concept and scope of the invention. 

What is claimed is:
 1. A seed, plant, plant part, or plant cell of inbred maize variety PH2DMA, representative seed of the variety having been deposited under ATCC accession number PTA-124043.
 2. The plant part of claim 1, wherein the plant part is an ovule or pollen.
 3. An F1 maize seed produced by crossing the plant or plant part of claim 1 with a different maize plant.
 4. A maize plant or plant part produced by growing the maize seed of claim
 3. 5. A method for producing a second maize plant, the method comprising applying plant breeding techniques to the plant or plant part of claim 4 to produce the second maize plant.
 6. A method for producing a second maize plant or plant part, the method comprising doubling haploid seed generated from a cross of the plant or plant part of claim 4 with an inducer variety, thereby producing the second maize plant or plant part.
 7. A method of making a commodity plant product comprising silage, starch, fat, syrup or protein, the method comprising producing the commodity plant product from the maize plant or plant part of claim
 4. 8. A method of producing a maize plant derived from the variety PH2DMA, comprising: a) crossing the plant of claim 1 with itself or a second plant to produce progeny seed; b) growing the progeny seed to produce a progeny plant and crossing the progeny plant with itself or a different plant to produce further progeny seed; and c) repeating step (b) for at least one additional generation to produce a maize plant derived from the variety PH2DMA.
 9. The derived maize plant produced by the method of claim 8, wherein the derived maize plant has the same morphological and physiological characteristics listed in Table 1 as inbred maize variety PH2DMA when grown under the same environmental conditions.
 10. A method comprising generating a molecular marker profile from nucleic acids isolated from the seed, plant, plant part, or plant cell of claim
 1. 11. A converted seed, plant, plant part or plant cell of inbred maize variety PH2DMA, representative seed of the maize variety PH2DMA having been deposited under ATCC accession number PTA-124043, wherein the converted seed, plant, plant part or plant cell comprises a locus conversion, and wherein the plant or a plant grown from the converted seed, plant part or plant cell comprises the locus conversion and otherwise has the same morphological and physiological characteristics of maize variety PH2DMA listed in Table 1 when grown under the same environmental conditions.
 12. The converted seed, plant, plant part or plant cell of claim 11, wherein the locus conversion confers a property selected from the group consisting of male sterility, site-specific recombination, abiotic stress tolerance, altered phosphorus, altered antioxidants, altered fatty acids, altered essential amino acids, altered carbohydrates, herbicide tolerance, insect resistance and disease resistance.
 13. An F1 maize seed produced by crossing the plant or plant part of claim 11 with a different maize plant.
 14. A maize plant or plant part produced by growing the seed of claim
 13. 15. A method for producing a second maize plant, the method comprising applying plant breeding techniques to the plant or plant part of claim 14 to produce the second maize plant.
 16. A method for producing a second maize plant or plant part, the method comprising doubling haploid seed generated from a cross of the plant or plant part of claim 14 with an inducer variety, thereby producing the second maize plant or plant part.
 17. A method of making a commodity plant product comprising silage, starch, fat, syrup or protein, the method comprising producing the commodity plant product from the maize plant or plant part of claim
 14. 18. A method of producing a maize plant derived from the variety PH2DMA, comprising: a) crossing the plant of claim 11 with itself or a second plant to produce progeny seed; b) growing the progeny seed to produce a progeny plant and crossing the progeny plant with itself or a different plant to produce further progeny seed; and c) repeating step (b) for at least one additional generation to produce a maize plant derived from the variety PH2DMA.
 19. The derived maize plant produced by the method of claim 18, wherein the derived maize plant has the same morphological and physiological characteristics listed in Table 1 as inbred maize variety PH2DMA when grown under the same environmental conditions.
 20. A method comprising generating a molecular marker profile from nucleic acids isolated from the seed, plant, plant part, or plant cell of claim
 11. 